Genomic variant #0001953086

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.11316742C>T
Reference Copied from the Exome Variant Server
DB-ID AMELX_000017
Frequency 2589/10563
Freq. EA 1475/6728
Freq. AA 1114/3835
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AMELX NM_001142.2 ?/? c.219C>T r.(=) p.(=)
ARHGAP6 NM_013427.2 ?/? c.589-43915G>A r.(=) p.(=)